Evidence map›Paper›PMID 39595537›Full record

ReviewBiomolecules2024

Cellular Senescence: A Bridge Between Diabetes and Microangiopathy.

Jiahui Liu, Buyu Guo, Qianqian Liu, Guomao Zhu, Yaqi Wang, Na Wang, Yichen Yang, Songbo Fu

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. SGLT2 Inhibition Attenuates Renal Tubular Senescence by Suppressing CTRP1-Mediated Glucotoxic Stress in Diabetic Kidney Disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. The Role of Renal Cell Senescence in Diabetic Kidney Disease: Mechanisms and Therapeutic Advances.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jiahui LiuThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Buyu GuoThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Qianqian LiuThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Guomao ZhuThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Yaqi WangThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Na WangThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Yichen YangThe First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Songbo FuDepartment of Endocrinology, The First Hospital of Lanzhou University, Lanzhou 730000, China.

Funding

Gansu Province Joint Research Fundation 23JRRA1490Gansu Province Natural Science Foundation 22JR5RA914Lanzhou Municipal Science and Technology Development Guidance Project 2019-ZD-38Lanzhou University 2024 College Students Innovation and Entrepreneurship Project 20240060002Lanzhou University 2024 College Students Innovation and Entrepreneurship Project 20240060086Lanzhou University 2024 College Students Innovation and Entrepreneurship Project 20240060088Lanzhou University 2024 College Students Innovation and Entrepreneurship Project 20240060133Lanzhou University 2024 College Students Innovation and Entrepreneurship Project 20240060146National Key R&D Program of China 2023YFC3503400
6 · The paper itself

Abstract

Cellular senescence is a state of permanent cell cycle arrest and plays an important role in many vascular lesions. This study found that the cells of diabetic patients have more characteristics of senescence, which may cause microvascular complications. Cell senescence, as one of the common fates of cells, links microangiopathy and diabetes. Cell senescence in a high-glucose environment can partially elucidate the mechanism of diabetic microangiopathy, and various types of cellular senescence induced by it can promote the progression of diabetic microangiopathy. Still, the molecular mechanism of microangiopathy-related cellular senescence has not yet been clearly studied. Building on recent research evidence, we herein summarize the fundamental mechanisms underlying the development of cellular senescence in various microangiopathies associated with diabetes. We gradually explain how cellular senescence serves as a key driver of diabetic microangiopathy. At the same time, the treatment of basic senescence mechanisms such as cellular senescence may have a great impact on the pathogenesis of the disease, may be more effective in preventing the development of diabetic microangiopathy, and may provide new ideas for the clinical treatment and prognosis of diabetic microangiopathy.

Indexed as

Cellular SenescenceDiabetic AngiopathiesAnimalsDiabetes MellitusHumanscellular senescencediabetes mellitusdiabetic cardiomyopathydiabetic nephropathydiabetic retinopathymicrovascular complications

Identifiers

PMID39595537
PMCPMC11591988

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.